MICROSCAN MICROSTREP PLUS, MODEL B1027-201— 510(k) K091949

Substantially Equivalent

Siemens Healthcare Diagnostics

FDA 510(k) clearance K091949 for MICROSCAN MICROSTREP PLUS, MODEL B1027-201, Substantially Equivalent on 2010-01-26. Applicant: Siemens Healthcare Diagnostics. Device class: 2.

Clearance details

Applicant
Siemens Healthcare Diagnostics
Product code
Code LTT
Device class
Class 2
Regulation
21 CFR 866.1640
Advisory panel
Microbiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
West Sacramento, CA, US
Download summary PDFView on FDA.gov ↗

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Recalls naming K091949

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K091949.

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